The Effect of Nicotine Delivery Rate on Reinforcement

Nicotine Clinical Trial

Official title:

The Effect of Nicotine Delivery Rate on Reinforcement

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03134339
• Other study ID #: 1609018390
• Status: Completed
• Phase: Early Phase 1
• Start date: January 5, 2017
• Est. completion date: January 29, 2018

Study information

• Verified date: October 2018
• Source: Yale University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The dose-effect curve to estimate a threshold delivery rate for reinforcement. The project addresses the FDA Center for Tobacco Products (CTP) interest #1: Nicotine dependence threshold among youth and adults and impact of nicotine reduction on tobacco product use behavior (e.g., topography, compensation, switching, multiple use, initiation, cessation and relapse). IV nicotine, in contrast to ECs, can deliver precise, reproducible dosing, which is necessary for accurately assessing dose-response and threshold effects. The estimated threshold for reinforcement will establish a benchmark for evaluating the addictive potential of ECs and other inhaled nicotine products.

Description:

A placebo-controlled study that will recruit male and female nicotine dependent smokers/EC users (n=18) to complete four separate experimental sessions. Each session will include one randomly assigned infusion that will be either saline or a single dose of nicotine (1 mg per 70 kg body weight) delivered at three different infusion rates, rapid, moderate or slow (0.24, 0.048 or 0.024 mcg per kg body weight per second). A total infusion duration of 10 min will be maintained during each session by adding saline infusions of variable duration after nicotine delivery. This will be achieved by two separate infusion pumps, one for saline and one for nicotine. For example, the rapid 0.24 mcg/kg/s condition will include a 1 min infusion of nicotine followed by a 9 min infusion of saline. The subjects will be blinded to the infusion pump procedures. The rapid delivery rate, which we have used in our prior studies, induces positive subjective drug effects and suppresses symptoms of nicotine withdrawal. The moderate delivery rate,0.048 mcg/kg/s, approximates the rate of nicotine intake encountered while smoking a typical cigarette over 5 min (4). The slowest nicotine delivery rate, 0.024mcg/kg/s, was chosen to approximate the rate of nicotine intake encountered while using a newer EC (5).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: January 29, 2018
• Est. primary completion date: January 29, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 30 Years

Eligibility

Inclusion Criteria:

1. Female and male smokers that smoke = 5 cigarettes per day for the past year

2. aged 18 to 30 years

3. urine cotinine levels > 100 ng/mL consistent with nicotine intake of an active smoker (23)

4. not seeking treatment at the time of the study for nicotine dependence

5. in good health as verified by medical history, screening examination, and screening laboratory tests

6. for women, not pregnant as determined by pregnancy screening, nor breast feeding, and using acceptable birth control methods.

Exclusion Criteria:

1. history of major medical or psychiatric disorders that the physician investigator deems as contraindicated for the subject to be in the study

2. regular use of psychotropic medication (antidepressants, antipsychotics, or anxiolytics)

3. current alcohol or substance dependence for any other recreational or prescription drugs other than nicotine

4. urine drug screening indicating recent illicit drugs use (with the exception of marijuana).

Related Conditions & MeSH terms

• Nicotine

Intervention

Drug:
• Nicotine saline 0.00mcg/kg/s
saline 0.00mcg/kg/s
• Nicotine 0.24 mcg/kg/s
nicotine 0.24 mcg/kg/s
• Nicotine 0.048 mcg/kg/s
nicotine 0.048 mcg/kg/s
• Nicotine 0.024 mcg/kg/s
nicotine 0.024 mcg/kg/s

Locations

Country	Name	City	State
United States	VA Hospital	West Haven	Connecticut

Sponsors (1)

Lead Sponsor	Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Peak Change on items of the Drug Effects Questionnaire (DEQ)	The peak change in the intensity of subjective effects as measured by the DEQ	up to 60 minutes post infusion